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This clinical handbook provides a clear and concise overview of how to recognize and diagnose inherited metabolic diseases. The reader is led through the diagnostic process from the identification of those features of an illness suggesting that it might be metabolic through the selection of appropriate laboratory investigation to a final diagnosis.
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Previews available in: English
Subjects
Diagnosis, Diagnosis, Differential, Diagnosis, Laboratory, Differential Diagnosis, Genetics, Inborn Errors Metabolism, Inborn errors of Metabolism, Laboratory Diagnosis, Metabolism, Inborn Errors, Metabolism, Inborn errors of, Therapy, Laboratory Techniques and Procedures, Erreurs innées du métabolisme, Diagnostic, Génétique, Thérapeutique, Diagnostic différentiel, Diagnostic laboratoire, Angeborene Krankheit, Stoffwechselkrankheit, Clinical Laboratory Techniques, Metabolic disorders in childrenShowing 3 featured editions. View all 11 editions?
Edition | Availability |
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1
A Clinical Guide to Inherited Metabolic Diseases
January 30, 2006, Cambridge University Press
Paperback
in English
- 3 edition
0521614996 9780521614993
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2
A Clinical Guide to Inherited Metabolic Diseases
July 15, 2002, Cambridge University Press
Paperback
in English
- 2 edition
0521890764 9780521890762
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3
A clinical guide to inherited metabolic diseases
1996, Cambridge University Press
in English
0521480647 9780521480642
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Book Details
First Sentence
"In his 1908 address to the Royal College of Physicians of London, Sir Archibald Garrod (1857-1936) coined the expression inborn error of metabolism to describe a group of disorders - alkaptonuria, benign pentosuria, albinism, and cystinuria -which ". . . apparently result from failure of some step or other in the series of chemical changes which constitute metabolism"."
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- Created April 29, 2008
- 15 revisions
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August 19, 2024 | Edited by MARC Bot | import existing book |
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